| Tag | Content |
|---|
EnhancerAtlas ID | HS108-37953 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr7:127887280-127888180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr7:127888002-127888013 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr7:127888002-127888013 | CTGAGTCACCC | - | 6.02 | | NFE2L1 | MA0089.2 | chr7:127887998-127888013 | TTTGCTGAGTCACCC | - | 6.88 | | Nr2f6(var.2) | MA0728.1 | chr7:127888129-127888144 | GAGGTCAGGAGTTCA | + | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 127888000 | 127888120 | | chr7 | 127887920 | 127888000 |
| Enhancer Sequence | CCACAGCTGC AGCGGGCCCC TGGGTCCTAC ATTTGCAGCC CTTTGTCTCT GAGCTCAGAC 60
TTCCAATTCC AAGCGGCAGC TGGGCAGGCT CACCAGCATG TCCAGCCAGT ACTAGGACAT 120
CAGCAGGAGC CCAACCACCT CTTTCCAAAA TCTCTCCTCA TGTCTCTCCT AGTTTCCATC 180
TCCATCCTTC TAGTCAGCCA GGCTGAAAAC ATTTGCTCCT CAGGGTGCAG AAGGGAAAGC 240
TTTGCCTCCC TTCCTGGTGC TCACTGCCCC TGCGATTCCA GCCCAAGCCC TCCCCGGCTC 300
CTCACCCTGG TGTCAGCTGG AAGCCACCAT CTCCTAAACC CACCTGTGTT CTTCCACCTC 360
TGCCAGGGCT GCCCTCTCCT CCACCTTCAC AAACTCAATT CCTACCCATT CTCAGGTCCC 420
TTATCAAATG CCATCTCCTC CATGATGCCT CCCTGATTCC CCTGCTGGAA ATAATGGTGA 480
TAACAGCTAA GGCATTGGGG TTGGCTACGT GCCAGGCAAG GAGTTGGCAC TTTACATGCT 540
TTATCTCATT TCAGCCACAT AACATCGACA GGTGGCATTA TGATTCATAT CATCCCCATC 600
TGATAGCCAG GAAAACTGAG TCCCAGAGAG GTTAGCCACT TTCCTAGGGC CCTGTGCTCT 660
GACTCAAGCA TAGCTCTGAG GAACTCTAGC ATTCATCAGT TTAAGCACCA TGACTTTCTT 720
TGCTGAGTCA CCCAAGGCAT TTCTTCATTT AAATGTTCTT CCTTGGCCAG GCGCAGTGGC 780
TCAGGCCCAA TGCGGTGGCT CACGCCTGTA ATCTCAACAC TTTGGGAGGC CGAGGTGGGC 840
AGATAATCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT 900
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